510(k) K222237
K222237 is an FDA 510(k) premarket notification submitted by Cala Health, Inc. for the device "Cala kIQ". The FDA issued a decision of Substantially Equivalent on Nov 22, 2022. The device falls under product code QBC (External Upper Limb Tremor Stimulator), a Class II device regulated under 21 CFR 882.5897. Cala Health, Inc. has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Nov 22, 2022
- Date Received
- Jul 26, 2022
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- External Upper Limb Tremor Stimulator
- Device Class
- Class II
- Regulation Number
- 882.5897
- Review Panel
- NE
- Submission Type
An external upper limb tremor stimulator is a prescription device which is placed externally on the upper limb and designed to aid in tremor symptom relief of the upper limb.